Site Manager Study Start UpReal World EvidenceEMEA basedJoin us on our exciting journey!IQVIA Real World Evidence (RWE) teams work with clients to help them collect and use real wo...
The Integration Management Office (IMO) is part of the GTO M&A Integration group. The IMO supplies tools, templates, processes and other means of support to the teams working to in...
Our multi sponsor, Site Management team is growing, join us on our mission to drive healthcare forward!Job Overview A CRA in our Site Management team will perform monitoring and si...
Senior Clinical Research Associate. Sponsor dedicatedHungary basedIQVIA is the Human Data Science Company oriented to drive human health outcomes forward.When you join IQVIA Hungar...
IQVIA Safety Operations team play an important part in the design, build and execution of end to end safety solutions for major pharmaceutical companies and their post market produ...
IQVIA Safety Operations team play an important part in the design, build and execution of end to end safety solutions for major pharmaceutical companies and their post market produ...
IQVIA Safety Operations team play an important part in the design, build and execution of end to end safety solutions for major pharmaceutical companies and their post market produ...
Associate Site Manager with FrenchReal World EvidenceHybrid. EMEAJoin us on our exciting journey!IQVIA Real World Evidence (RWE) teams work with clients to help them collect and us...
Job OverviewWe are looking to hire a (Sr) Site Activation Coordinator to perform administrative tasks at a country level in accordance with applicable local and or international re...
Job OverviewManage and support the operational elements and execution of studies and or programs to ensure delivery. time and quality resulting in strong financial performance and ...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts...
Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and or international regulations, standard operatin...
The IQVIA Cardiovascular Center of Excellence, a hub of clinical innovation, is growing! We are looking for exceptional Board Certified physicians to join our team as a Medical Str...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a C...
Office based position in Budapest, Hungary.Job OverviewUnder general supervision, provide remote second tier Information Technology (IT) support to end users, to restore service an...
Job OverviewThis position is responsible for providing line management to an assigned data management team. This role is also responsible for delivering strategic solutions and pro...
Job Description. Provide line and functional management of Data Management technical experts, with a team size of around 15 20 people.Manage and prioritize resource assignments, as...
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical tri...
RESPONSIBILITIESProvide compensation program management and execution including but not limited to. base pay and variable administration, year end performance and pay management pr...
Job OverviewThe medical department consists of a Chief Medical Officer, Medical Directors, medical writers, and safety associates. The Medical Director provides medical and scienti...
Country Site ActivationJoin us on our exciting journey!IQVIA's Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure pa...
Who are we?We are the creators of ClinSpark , the world's first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (now known as 'IQVIA Clinical eS...
This unique role within IQVIA lends itself to a technically minded Project Manager with strong communication skills and SDTM knowledge. Having experience with SAS programming will ...
This unique role within IQVIA lends itself to a technically minded Project Manager with strong communication skills and SDTM knowledge. Having experience with SAS programming will ...
IQVIA is looking to hire a Contract Negotiator based in Hungary sponsor dedicated. Job OverviewAs a Contract Negotiator you will develop the global contracting strategy and support...
Job OverviewThe Senior Manager, Clinical Supply Chain Management supervises, manages and provides oversight of Clinical Supply Chain Managers to ensure effective delivery of clinic...